Adolescent Master Protocol (AMP)
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|ClinicalTrials.gov Identifier: NCT01418014|
Recruitment Status : Active, not recruiting
First Posted : August 16, 2011
Last Update Posted : January 31, 2018
The advances in treatment to prevent maternal HIV transmission to neonates have been groundbreaking. As a result, the number of new perinatally-infected children in the U.S. is now small. Subsequent improvements in the treatment of HIV-infected infants and children have been equally remarkable, ensuring that most previously infected American children have survived and are approaching adolescence. In addition, the number of HIV-infected adolescents worldwide is growing substantially in both resource-poor countries and in countries with increasing levels of health care. Therefore, there is a global cohort of children who have been living with HIV infection since birth who are aging into adolescence. Little is definitively known about the impact of HIV infection and its treatment on the maturation process in these children.
AMP is a prospective cohort study designed to define the impact of HIV infection and antiretroviral therapy on pre-adolescents and adolescents with perinatal HIV infection. Domains to be investigated include growth and sexual maturation, metabolic risk factors for cardiovascular disease, cardiac function, bone health, neurologic, neurodevelopment, language, hearing and behavioral function, and sexually transmitted infections (STI).
|Condition or disease|
The primary objectives of AMP are:
- To define the impact of HIV infection and ART on growth and pubertal development (and their hormonal regulation), along with the cognitive, academic, and social development, of pre-adolescents and adolescents with perinatal HIV infection as they move through adolescence into adulthood.
- To identify infectious and non-infectious complications of HIV disease, including the toxicities of antiretroviral therapy (ART).
- Cognitive and behavioral changes over time, including medication adherence, family and social function, and high risk behaviors such as risky sexual behavior, licit and illicit drug use, and alcohol use;
- Changes in language and hearing;
- Changes in glucose metabolism, body composition, and bone mineralization;
- Changes in lipid metabolism and other risk factors for cardiovascular disease;
- Risk factors for secondary transmission of HIV; and
- The occurrence and clinical course of cervical HPV infections among females.
The domain-specific aims of AMP are:
- Growth and sexual maturation: To longitudinally track growth and sexual maturation and the factors that influence growth and maturation in HIV-infected children when compared to HIV-exposed but uninfected children.
- Metabolic risk factors for cardiovascular disease: To characterize the emergence of abnormal glucose metabolism, lipid abnormalities, body composition and other risk factors for cardiovascular disease and identify the contributing influences in HIV-infected children when compared to HIV-exposed but uninfected children.
- Cardiac function: To estimate the prevalence of cardiac structural and functional abnormalities in HIV-infected children and youth when compared to HIV-exposed but uninfected children.
- Bone mineral density: To estimate the differences in bone mineral density of HIV-infected children when compared to HIV-exposed but uninfected children and to identify factors contributing to abnormal bone mineralization.
Neurologic, neurodevelopment, language, and behavioral function:
- To examine cognitive and behavioral outcomes of HIV-infected children and adolescents, including high risk behaviors such as risky sexual behavior, licit and illicit drug use, and alcohol use, neurodevelopmental impairment, school achievement and to compare them with an HIV-exposed but uninfected control cohort.
- To examine non-adherence to antiretroviral therapy and predictors of non-adherence among HIV-infected children receiving ART.
- To examine family and psychosocial factors associated with emotional and behavioral problems.
Adolescent gynecology and STI infection:
- To evaluate the incidence of and risk factors for acquiring STIs/vaginal infections (C. trachomatis, N. gonorrhea, T. vaginalis, syphilis, genital warts, HPV, and HSV) for males and females, and in addition bacterial vaginosis for females.
- To evaluate the incidence, predictors, and outcomes of pregnancy.
|Study Type :||Observational|
|Actual Enrollment :||678 participants|
|Official Title:||Adolescent Master Protocol|
|Study Start Date :||March 2007|
|Estimated Primary Completion Date :||July 2020|
|Estimated Study Completion Date :||July 2020|
Perinatally HIV-infected adolescents from 7 years of age (7th birthday) up to but not including the 16th birthday at enrollment, engaged in care with ART treatment history available.
HIV-uninfected adolescents from 7 years of age (7th birthday) up to but not including the 16th birthday at enrollment born to HIV-infected mothers.
- Abnormal growth [ Time Frame: Annually for 10 years ]Assessed via measurement of height, weight, skinfold thickness, mid-upper arm and waist and hip circumference, nutrition and physical activity questionnaires ; subjects meeting growth trigger based on height measurements also have the following laboratory assessments: IGF-I, IGFBP-3, and GHBP. A growth hormone stimulation test may also be required at the recommendation of the endocrinologist.
- Delayed sexual maturation [ Time Frame: Annually for 10 years except if subject reaches Tanner Stage 5 ]Assessed via tanner staging; subjects meeting the growth trigger based on the results of the tanner staging will also have the following laboratory assessments: morning LH, FSH, estradiol, and testosterone
- Abnormal bone mineral density [ Time Frame: Two DXAs, two years apart, per HIV-infected subject; one DXA per uninfected subject; X-ray at same time as DXA unless subject Tanner Stage 5 ]Assessed via DXA scan and x-ray for bone age; subjects meeting the BMD trigger based on the DXA also have the following laboratory assessments: TSH, calcium, 25-hydroxy-vitamin D, bone-specific alkaline, N-terminal telopeptide of type I collagen phosphatase, and PTH in real time and repository specimens for assay of pro-inflammatory cytokines (IL-1, IL-6, TNF-a)
- Dyslipidemia [ Time Frame: Annually for 10 years ]Assessed via lipid testing; subjects meeting the metabolic trigger based on the results of the lipid tests also have the following measurements: endothelial dysfunction (I, E, P-selectins: V, I-CAM-1, endothelin-1, hs-CRP, homocysteine, apolipoprotein B, lipoprotein (a), and vWF antigen)
- Cardiac abnormalities [ Time Frame: Measured once per subject until study reached 400 echocardiograms ]Assessed through the administration of echocardiograms and serum biomarkers (ProBNP)
- Hearing dysfunction [ Time Frame: Once per subject. ]Assessed via audiologic evaluation conducted by an audiologist.
- Language dysfunction [ Time Frame: Annually for 10 years ]Assessed using the Woodcock and CELF IV language tests
- Neurodevelopmental abnormalities [ Time Frame: Annually for 10 years ]Assessed via the following neurodevelopmental tests: WISC IV, WAIS IV, BRIEF, Children's Color Trails Test, Trail Making Tests, WIAT-II screen, ABAS, Parent Child Relationship Inventory, BASC-2, Quality of Life Interview, Stressful Life Events Questionnaire, Monitoring the Future
- Substance Use [ Time Frame: Annually starting at a minimum of 10 years of age for 10 years ]The assessment of sexual activity is conducted using an Audio Computer Assisted Survey Instrument (ACASI). ACASI uses computer and voice recordings so that the participant hears (through headphones) and sees (on the screen) each question and response list. The use of ACASI is proven to minimize response bias due to the presence of an interviewer.
- Sexual Activity [ Time Frame: Annually starting at a minimum of 10 years of age for 10 years ]The assessment of substance use is conducted using an Audio Computer Assisted Survey Instrument (ACASI). ACASI uses computer and voice recordings so that the participant hears (through headphones) and sees (on the screen) each question and response list. The use of ACASI is proven to minimize response bias due to the presence of an interviewer.
- Pregnancy [ Time Frame: Annually for 10 years ]Assessed via medical record review to record incidents of pregnancy
- Sexually Transmitted Infection [ Time Frame: Annually for 10 years ]Assessed via medical record review to record results of clinically conducted STI and Pap testing and pelvic exams
- Mitochondrial dysfunction [ Time Frame: Annually for 10 years ]Assessed via measurement of serum lactate levels, OXPHO immunoassays, mitochondrial specific oxidative stress, mtDNA copies/cell, mrRNA transcripts
- Lactic acidosis [ Time Frame: Annually for 10 years ]Assessed through the measurement of blood lactate levels using a point-of-care lactate measuring device; a single venous lactate measurement will be conducted in cases where the POC lactate measure is elevated
- Renal abnormalities [ Time Frame: Annually for 10 years ]Assessed through the following laboratory measurements: chemistry panel, urinalysis, protein/creatinine ratio, dip stick urine test
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01418014
|United States, California|
|University of California San Diego|
|La Jolla, California, United States, 92093|
|United States, Colorado|
|University of Colorado Denver Health Sciences Center|
|Aurora, Colorado, United States, 80045|
|United States, Florida|
|Children's Diagnostic and Treatment Center|
|Fort Lauderdale, Florida, United States, 33316|
|University of Miami|
|Miami, Florida, United States, 33136|
|United States, Illinois|
|Ann and Robert H. Lurie Children's Hospital|
|Chicago, Illinois, United States, 60614|
|United States, Louisiana|
|Tulane University Health Sciences Center|
|New Orleans, Louisiana, United States, 70112|
|United States, Maryland|
|University of Maryland|
|Baltimore, Maryland, United States, 21201|
|United States, Massachusetts|
|Children's Hospital Boston|
|Boston, Massachusetts, United States, 02115|
|United States, New Jersey|
|Rutgers - New Jersey Medical School|
|Newark, New Jersey, United States, 07101|
|United States, New York|
|Bronx Lebanon Hospital Center|
|Bronx, New York, United States, 10457|
|Jacobi Medical Center|
|Bronx, New York, United States, 10461|
|United States, Pennsylvania|
|St. Christopher's Hospital for Children|
|Philadelphia, Pennsylvania, United States, 19134|
|United States, Tennessee|
|St. Jude Children's Research Hospital|
|Memphis, Tennessee, United States, 38105|
|United States, Texas|
|Baylor College of Medicine|
|Houston, Texas, United States, 77030|
|San Juan Research Hospital|
|San Juan, Puerto Rico, 00936|
|Principal Investigator:||George R Seage III, ScD, MPH||Harvard School of Public Health|
|Principal Investigator:||Russell Van Dyke, M.D.||Tulane University School of Medicine|